ON CARBOFURAN posits of the technical and formulated material and in water solution. The major identified photoproducts arise through established oxidative and hydrolytic mechanisms. Oxidation of the phenyl-S-methyl sulfur to sulfoxide and sulfone derivatives appeared to be the initial step in the degradation of 9306. Comparable photochemical oxidation of thioether moieties is known for both OP (Wendel and Bull, 1970) and carbamate (Abdel-Wahab et al., 1966) insecticides. Likewise, oxidative desulfuration and aryl ester cleavage of OP insecticides are previously reported photochemical pathways (Koivistoinen and Merilainen, 1962; Ohkawa et al., 1974).The identified photoproducts of 9306 (Figure 2), which are formed through straightforward oxidative and hydrolytic reactions, are clearly not the terminal photodegradation residues to be expected in the environment because more polar products are rapidly generated both on surfaces and in water solution. While these polar derivatives remain uncharacterized, studies with rats indicate that they will not likely result in appreciable toxicological hazards to mammals. The compounds were rapidly excreted by rats and were not retained in the tissues. These studies thus indicate that 9306 will be of short persistence in the environment, and that the persisting terminal residues will likely be of little toxicological significance. LITERATURE CITED